A 3-Year Overall Survival Update From a Phase 2 Study of Chemoselection With DCF and Subsequent Conversion Surgery for Locally Advanced Unresectable Esophageal Cancer.


Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 13 03 2019
pubmed: 4 8 2019
medline: 30 9 2020
entrez: 4 8 2019
Statut: ppublish

Résumé

A multicenter phase 2 trial analysed chemoselection with docetaxel plus 5-fluorouracil and cisplatin (DCF) induction chemotherapy (ICT) and subsequent conversion surgery (CS) for locally advanced unresectable esophageal cancer. This study presents updated 3-year analyses to further characterize the impact of DCF-ICT followed by CS. Esophageal cancer patients with clinical T4 disease, unresectable supraclavicular lymph node metastasis, or both were eligible for this study. The treatment starts with DCF-ICT, followed by CS if the cancer is resectable, or by concurrent chemoradiation if it is not resectable. This updated analysis presents 3-year overall survival (OS), 3-year progression-free survival (PFS), and pattern of relapse. The median follow-up period for the patients surviving without death was 39.3 months. The estimated 1-year OS was 66.7%, and the lower limit of the 80% confidence interval (CI) was 54.6%. The estimated 3-year OS was 46.6% (95% CI 34.2-63.5%). The OS for the patients who underwent R0 resection (n = 19) was significantly longer than for those who did not (3-year OS: 71.4% vs. 30.1%). The estimated 1-year PFS was 50.6%, and the 3-year PFS was 39.6%. The PFS for R0 was significantly longer than for non-R0 (3-year PFS: 61.3% vs 25.0%). Recurrence or progression at the primary site was observed in 31% of the non-R0 group. The rate of distant metastasis did not differ significantly between the non-R0 and R0 groups (21% vs 16%). Long-term follow-up evaluation confirmed that DCF chemoselection aimed at CS is feasible and promising in terms of survival for patients with locally advanced esophageal cancer.

Sections du résumé

BACKGROUND BACKGROUND
A multicenter phase 2 trial analysed chemoselection with docetaxel plus 5-fluorouracil and cisplatin (DCF) induction chemotherapy (ICT) and subsequent conversion surgery (CS) for locally advanced unresectable esophageal cancer. This study presents updated 3-year analyses to further characterize the impact of DCF-ICT followed by CS.
METHODS METHODS
Esophageal cancer patients with clinical T4 disease, unresectable supraclavicular lymph node metastasis, or both were eligible for this study. The treatment starts with DCF-ICT, followed by CS if the cancer is resectable, or by concurrent chemoradiation if it is not resectable. This updated analysis presents 3-year overall survival (OS), 3-year progression-free survival (PFS), and pattern of relapse.
RESULTS RESULTS
The median follow-up period for the patients surviving without death was 39.3 months. The estimated 1-year OS was 66.7%, and the lower limit of the 80% confidence interval (CI) was 54.6%. The estimated 3-year OS was 46.6% (95% CI 34.2-63.5%). The OS for the patients who underwent R0 resection (n = 19) was significantly longer than for those who did not (3-year OS: 71.4% vs. 30.1%). The estimated 1-year PFS was 50.6%, and the 3-year PFS was 39.6%. The PFS for R0 was significantly longer than for non-R0 (3-year PFS: 61.3% vs 25.0%). Recurrence or progression at the primary site was observed in 31% of the non-R0 group. The rate of distant metastasis did not differ significantly between the non-R0 and R0 groups (21% vs 16%).
CONCLUSIONS CONCLUSIONS
Long-term follow-up evaluation confirmed that DCF chemoselection aimed at CS is feasible and promising in terms of survival for patients with locally advanced esophageal cancer.

Identifiants

pubmed: 31376034
doi: 10.1245/s10434-019-07654-8
pii: 10.1245/s10434-019-07654-8
doi:

Substances chimiques

Docetaxel 15H5577CQD
Cisplatin Q20Q21Q62J
Fluorouracil U3P01618RT

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

460-467

Subventions

Organisme : National Cancer Center Research and Development Fund
ID : 26-A-4

Auteurs

Tomoya Yokota (T)

Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Shizuoka, Japan. t.yokota@scchr.jp.

Ken Kato (K)

Gastrointestinal Oncology Division, National Cancer Center Hospital, Tokyo, Japan.

Yasuo Hamamoto (Y)

Division of Gastroenterology and Hepatology, Keio University School of Medicine, Tokyo, Japan.

Yasuhiro Tsubosa (Y)

Division of Esophageal Surgery, Shizuoka Cancer Center, Shizuoka, Japan.

Hirofumi Ogawa (H)

Division of Radiation Oncology, Shizuoka Cancer Center, Shizuoka, Japan.

Yoshinori Ito (Y)

Department of Radiation Oncology, National Cancer Center Hospital, Tokyo, Japan.

Hiroki Hara (H)

Department of Gastroenterology, Saitama Cancer Center, Saitama, Japan.

Takashi Ura (T)

Department of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.

Takashi Kojima (T)

Department of Gastroenterology, National Cancer Center Hospital East, Chiba, Japan.

Keisho Chin (K)

Department of Gastroenterology, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.

Shuichi Hironaka (S)

Clinical Trial Promotion Department, Chiba Cancer Center, Chiba, Japan.

Takayuki Kii (T)

Cancer Chemotherapy Center, Osaka Medical College Hospital, Osaka, Japan.

Yasushi Kojima (Y)

Department of Gastroenterology, National Center for Global Health and Medicine, Tokyo, Japan.

Yasunori Akutsu (Y)

Department of Frontier Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.

Hisayuki Matsushita (H)

Department of Surgery, Tochigi Cancer Center, Tochigi, Japan.

Kentaro Kawakami (K)

Department of Medical Oncology, Tochigi Cancer Center, Tochigi, Japan.

Keita Mori (K)

Clinical Trial Coordination Office, Shizuoka Cancer Center, Shizuoka, Japan.

Takashi Makiuchi (T)

Clinical Data Management, Clinical Research Data Center, National Cancer Center Hospital, Tokyo, Japan.

Rie Nagumo (R)

Clinical Data Management, Clinical Research Data Center, National Cancer Center Hospital, Tokyo, Japan.

Yuko Kitagawa (Y)

Department of Surgery, Keio University School of Medicine, Tokyo, Japan.

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Classifications MeSH